Cytokines, POD, Health Status, Older Hip Fracture

NCT ID: NCT05096507

Last Updated: 2022-08-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-06-06

Study Completion Date

2023-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

An investigation of the change in inflammation marker levels across hip fracture surgery and an exploration of any association with change in self reported health status and incidence of postoperative delirium

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Postoperative Delirium Hip Fracture Surgery Older People

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Study group

People age 65 years and older undergoing primary hip fracture surgery

Hip fracture Surgery (Primary)

Intervention Type PROCEDURE

Surgery for primary hip fracture requiring general or neuro-axial anaesthesia

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Hip fracture Surgery (Primary)

Surgery for primary hip fracture requiring general or neuro-axial anaesthesia

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age ≥ 65 years old
* Admitted for primary hip fracture surgery

Exclusion Criteria

* Preoperative cognitive impairment
* History of neurosurgery, neurologic diseases or head trauma
* Current systemic bacterial or viral infection
* Complex or multiple injuries
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Nottingham

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Iain Moppett, DM

Role: PRINCIPAL_INVESTIGATOR

University of Nottingham

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Queen's Medical Centre

Nottingham, , United Kingdom

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

United Kingdom

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Abiodun Noah, FRCA

Role: CONTACT

01158231011

Iain Moppett, DM

Role: CONTACT

01158230959

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Jennifer Boston

Role: primary

01159249924

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

21052

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Hip Fracture Surgery in Elderly Patients
NCT01199276 COMPLETED PHASE2
Frailty and Postoperative Shock
NCT02669927 COMPLETED